Details
Stereochemistry | ACHIRAL |
Molecular Formula | C5H6N2 |
Molecular Weight | 94.1145 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=CC=NC=C1
InChI
InChIKey=NUKYPUAOHBNCPY-UHFFFAOYSA-N
InChI=1S/C5H6N2/c6-5-1-3-7-4-2-5/h1-4H,(H2,6,7)
Molecular Formula | C5H6N2 |
Molecular Weight | 94.1145 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionCurator's Comment: description was created based on several sources, including
https://www.drugs.com/cdi/dalfampridine.html | https://clinicaltrials.gov/ct2/show/NCT01356940 | https://www.ncbi.nlm.nih.gov/pubmed/22497693 | https://www.ncbi.nlm.nih.gov/pubmed/15084131
Curator's Comment: description was created based on several sources, including
https://www.drugs.com/cdi/dalfampridine.html | https://clinicaltrials.gov/ct2/show/NCT01356940 | https://www.ncbi.nlm.nih.gov/pubmed/22497693 | https://www.ncbi.nlm.nih.gov/pubmed/15084131
Dalfampridine is a potassium channel blocker, used as a research tool in characterizing subtypes of the potassium channel. Dalfampridine has also been used as a drug, to manage some of the symptoms of multiple sclerosis, and is indicated for symptomatic improvement of walking in adults with several variations of the disease. The mechanism by which dalfampridine exerts its therapeutic effect has not been fully elucidated. Dalfampridine is a broad spectrum potassium channel blocker. In animal studies, dalfampridine has been shown to increase conduction of action potentials in demyelinated axons through inhibition of potassium channels.
CNS Activity
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL4633 Sources: https://www.ncbi.nlm.nih.gov/pubmed/15084131 |
195.0 µM [Kd] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | AMPYRA Approved UseAMPYRA (dalfampridine) is indicated as a treatment to improve walking in patients with multiple sclerosis (MS). This was demonstrated by an increase in walking speed [see Clinical Studies (14) Launch Date2010 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
23.77 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22058101/ |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
DALFAMPRIDINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
246.48 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22058101/ |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
DALFAMPRIDINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
0.16 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22058101/ |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
DALFAMPRIDINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
Funbound
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
97% EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/22058101/ |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
DALFAMPRIDINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
Doses
Dose | Population | Adverse events |
---|---|---|
10 mg 2 times / day multiple, oral Recommended Dose: 10 mg, 2 times / day Route: oral Route: multiple Dose: 10 mg, 2 times / day Sources: Page: p.3 |
unhealthy, 52.1 ± 8.8 n = 269 Health Status: unhealthy Condition: Multiple sclerosis Age Group: 52.1 ± 8.8 Sex: M+F Population Size: 269 Sources: Page: p.3 |
Disc. AE: Seizure, Myocardial infarction... AEs leading to discontinuation/dose reduction: Seizure (1.1%) Sources: Page: p.3Myocardial infarction (1.1%) |
300 mg single, oral Overdose Dose: 300 mg Route: oral Route: single Dose: 300 mg Sources: Page: p.3 |
unhealthy n = 1 Health Status: unhealthy Condition: Multiple sclerosis Population Size: 1 Sources: Page: p.3 |
Disc. AE: Weakness, Consciousness decreased... AEs leading to discontinuation/dose reduction: Weakness Sources: Page: p.3Consciousness decreased Memory loss Hypophonia Structural brain disorders NEC |
40 mg single, oral Overdose Dose: 40 mg Route: oral Route: single Dose: 40 mg Sources: Page: p.3 |
unhealthy n = 1 Health Status: unhealthy Condition: Multiple sclerosis Sex: F Population Size: 1 Sources: Page: p.3 |
Disc. AE: Complex partial seizures, Confusion... AEs leading to discontinuation/dose reduction: Complex partial seizures Sources: Page: p.3Confusion |
60 mg single, oral Overdose Dose: 60 mg Route: oral Route: single Dose: 60 mg Sources: Page: p.3 |
unhealthy n = 1 Health Status: unhealthy Condition: Multiple sclerosis Population Size: 1 Sources: Page: p.3 |
Disc. AE: Mental state abnormal... AEs leading to discontinuation/dose reduction: Mental state abnormal Sources: Page: p.3 |
10 mg 2 times / day multiple, oral Recommended Dose: 10 mg, 2 times / day Route: oral Route: multiple Dose: 10 mg, 2 times / day Sources: Page: p.2 |
unhealthy n = 400 Health Status: unhealthy Condition: Multiple sclerosis Population Size: 400 Sources: Page: p.2 |
Disc. AE: Headache, Balance disorder... AEs leading to discontinuation/dose reduction: Headache (0.5%) Sources: Page: p.2Balance disorder (0.5%) Dizziness (0.5%) Confusional state (0.5%) |
10 mg 2 times / day multiple, oral Recommended Dose: 10 mg, 2 times / day Route: oral Route: multiple Dose: 10 mg, 2 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Multiple sclerosis Sources: Page: p.1 |
Disc. AE: Seizures... AEs leading to discontinuation/dose reduction: Seizures Sources: Page: p.1 |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Myocardial infarction | 1.1% Disc. AE |
10 mg 2 times / day multiple, oral Recommended Dose: 10 mg, 2 times / day Route: oral Route: multiple Dose: 10 mg, 2 times / day Sources: Page: p.3 |
unhealthy, 52.1 ± 8.8 n = 269 Health Status: unhealthy Condition: Multiple sclerosis Age Group: 52.1 ± 8.8 Sex: M+F Population Size: 269 Sources: Page: p.3 |
Seizure | 1.1% Disc. AE |
10 mg 2 times / day multiple, oral Recommended Dose: 10 mg, 2 times / day Route: oral Route: multiple Dose: 10 mg, 2 times / day Sources: Page: p.3 |
unhealthy, 52.1 ± 8.8 n = 269 Health Status: unhealthy Condition: Multiple sclerosis Age Group: 52.1 ± 8.8 Sex: M+F Population Size: 269 Sources: Page: p.3 |
Consciousness decreased | Disc. AE | 300 mg single, oral Overdose Dose: 300 mg Route: oral Route: single Dose: 300 mg Sources: Page: p.3 |
unhealthy n = 1 Health Status: unhealthy Condition: Multiple sclerosis Population Size: 1 Sources: Page: p.3 |
Hypophonia | Disc. AE | 300 mg single, oral Overdose Dose: 300 mg Route: oral Route: single Dose: 300 mg Sources: Page: p.3 |
unhealthy n = 1 Health Status: unhealthy Condition: Multiple sclerosis Population Size: 1 Sources: Page: p.3 |
Memory loss | Disc. AE | 300 mg single, oral Overdose Dose: 300 mg Route: oral Route: single Dose: 300 mg Sources: Page: p.3 |
unhealthy n = 1 Health Status: unhealthy Condition: Multiple sclerosis Population Size: 1 Sources: Page: p.3 |
Structural brain disorders NEC | Disc. AE | 300 mg single, oral Overdose Dose: 300 mg Route: oral Route: single Dose: 300 mg Sources: Page: p.3 |
unhealthy n = 1 Health Status: unhealthy Condition: Multiple sclerosis Population Size: 1 Sources: Page: p.3 |
Weakness | Disc. AE | 300 mg single, oral Overdose Dose: 300 mg Route: oral Route: single Dose: 300 mg Sources: Page: p.3 |
unhealthy n = 1 Health Status: unhealthy Condition: Multiple sclerosis Population Size: 1 Sources: Page: p.3 |
Complex partial seizures | Disc. AE | 40 mg single, oral Overdose Dose: 40 mg Route: oral Route: single Dose: 40 mg Sources: Page: p.3 |
unhealthy n = 1 Health Status: unhealthy Condition: Multiple sclerosis Sex: F Population Size: 1 Sources: Page: p.3 |
Confusion | Disc. AE | 40 mg single, oral Overdose Dose: 40 mg Route: oral Route: single Dose: 40 mg Sources: Page: p.3 |
unhealthy n = 1 Health Status: unhealthy Condition: Multiple sclerosis Sex: F Population Size: 1 Sources: Page: p.3 |
Mental state abnormal | Disc. AE | 60 mg single, oral Overdose Dose: 60 mg Route: oral Route: single Dose: 60 mg Sources: Page: p.3 |
unhealthy n = 1 Health Status: unhealthy Condition: Multiple sclerosis Population Size: 1 Sources: Page: p.3 |
Balance disorder | 0.5% Disc. AE |
10 mg 2 times / day multiple, oral Recommended Dose: 10 mg, 2 times / day Route: oral Route: multiple Dose: 10 mg, 2 times / day Sources: Page: p.2 |
unhealthy n = 400 Health Status: unhealthy Condition: Multiple sclerosis Population Size: 400 Sources: Page: p.2 |
Confusional state | 0.5% Disc. AE |
10 mg 2 times / day multiple, oral Recommended Dose: 10 mg, 2 times / day Route: oral Route: multiple Dose: 10 mg, 2 times / day Sources: Page: p.2 |
unhealthy n = 400 Health Status: unhealthy Condition: Multiple sclerosis Population Size: 400 Sources: Page: p.2 |
Dizziness | 0.5% Disc. AE |
10 mg 2 times / day multiple, oral Recommended Dose: 10 mg, 2 times / day Route: oral Route: multiple Dose: 10 mg, 2 times / day Sources: Page: p.2 |
unhealthy n = 400 Health Status: unhealthy Condition: Multiple sclerosis Population Size: 400 Sources: Page: p.2 |
Headache | 0.5% Disc. AE |
10 mg 2 times / day multiple, oral Recommended Dose: 10 mg, 2 times / day Route: oral Route: multiple Dose: 10 mg, 2 times / day Sources: Page: p.2 |
unhealthy n = 400 Health Status: unhealthy Condition: Multiple sclerosis Population Size: 400 Sources: Page: p.2 |
Seizures | Disc. AE | 10 mg 2 times / day multiple, oral Recommended Dose: 10 mg, 2 times / day Route: oral Route: multiple Dose: 10 mg, 2 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Multiple sclerosis Sources: Page: p.1 |
Overview
CYP3A4 | CYP2C9 | CYP2D6 | hERG |
---|---|---|---|
OverviewOther
Drug as perpetrator
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
no | ||||
Page: 41, (ClinPharm) 28, 50 |
no | |||
Page: 41, (ClinPharm) 28, 50 |
no | |||
no | ||||
Page: 41, (ClinPharm) 28, 50 |
no | |||
no | ||||
Page: 41, (ClinPharm) 28, 50 |
no | |||
Page: 41, (ClinPharm) 28, 50 |
no | |||
no | ||||
Page: 41, (ClinPharm) 28, 50 |
no | |||
Page: 41, (ClinPharm) 28, 50 |
no | |||
no | ||||
no | ||||
Page: 41, (ClinPharm) 28, 50 |
no | |||
no | ||||
Page: 32; Pharmacological Reviews December 2005, 57 (4) 473-508 |
weak [IC50 195 uM] | |||
Page: 33; Pharmacological Reviews December 2005, 57 (4) 473-508 |
weak [IC50 270 uM] |
Drug as victim
Tox targets
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
PubMed
Title | Date | PubMed |
---|---|---|
Okadaic acid and cyclosporin A modulate [(3)H]GABA release from rat brain synaptosomes. | 2001 Apr |
|
Syntheses of the first amine-dicarboxyboranes and their bis(methylester) and bis(N-ethylamide) derivatives. | 2001 Apr 9 |
|
General rules for the packing of hydrogen-bonded crystals as derived from the analysis of squaric acid anions: aminoaromatic nitrogen base co-crystals. | 2001 Aug |
|
Large-conductance calcium-activated potassium channels in neonatal rat intracardiac ganglion neurons. | 2001 Feb |
|
Pharmacological properties of excitation-contraction mechanisms in isolated mouse left atria. | 2001 Feb |
|
Modulation of diaphragm action potentials by K(+) channel blockers. | 2001 Feb |
|
Swim stress alters the behavioural response of mice to GABA-related and some GABA-unrelated convulsants. | 2001 Feb |
|
Facilitated glutamatergic transmission in the striatum of D2 dopamine receptor-deficient mice. | 2001 Feb |
|
The effect of acidosis on the ECG of the rat heart. | 2001 Jan |
|
Three types of K(+) currents in murine osteocyte-like cells (MLO-Y4). | 2001 Jan |
|
Development and validation of a capillary electrophoresis assay for the determination of 3,4-diaminopyridine and 4-aminopyridine including related substances. | 2001 Jan 12 |
|
Neurogenic bladder in Lambert-Eaton myasthenic syndrome and its response to 3,4-diaminopyridine. | 2001 Jan 15 |
|
K(ATP) channel blockers selectively interact with A(1)-adenosine receptor mediated modulation of acetylcholine release in the rat hippocampus. | 2001 Jan 19 |
|
Alterations in a redox oxygen sensing mechanism in chronic hypoxia. | 2001 Jun |
|
Synchronized Ca2+ signals mediated by Ca2+ action potentials in the hippocampal neuron network in vitro. | 2001 Jun |
|
Mechanisms underlying presynaptic facilitatory effect of cyclothiazide at the calyx of Held of juvenile rats. | 2001 Jun 1 |
|
Anticonvulsant properties and bio-guided isolation of palmitone from leaves of Annona diversifolia. | 2001 Mar |
|
Three types of depolarization-activated potassium currents in acutely isolated mouse vestibular neurons. | 2001 Mar |
|
Influence of admixed carboxymethylcellulose on release of 4-aminopyridine from hydroxypropyl methylcellulose matrix tablets. | 2001 Mar 23 |
|
Time-dependent distribution and neuronal localization of c-fos protein in the rat hippocampus following 4-aminopyridine seizures. | 2001 May |
|
Targeted replacement of KV1.5 in the mouse leads to loss of the 4-aminopyridine-sensitive component of I(K,slow) and resistance to drug-induced qt prolongation. | 2001 May 11 |
|
Stretch-dependent potassium channels in murine colonic smooth muscle cells. | 2001 May 15 |
|
Oxygen dilation in fetal pulmonary arterioles: role of K(+) channels. | 2001 May 15 |
|
BTS 72664-- a novel CNS drug with potential anticonvulsant, neuroprotective, and antimigraine properties. | 2001 Summer |
Patents
Sample Use Guides
The maximum recommended dose of AMPYRA is one 10 mg tablet twice daily, taken with or without food, and should not be exceeded.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26946488
At DIV25, the differentiating cells were re-seeded to Matrigel coated 12-mm glass coverslips in densities of 400,000 cells per well. Media was replaced completely the next day by fresh maturation media. Media containing either 100 mM 4-Aminopyridine diluted in DMSO or the equivalent amount DMSO only was given to the cells 72 hours before the start of week 7 (DIV42) and lasted until the cells were analyzed during week 7. Half the media was replaced every third day. Final electrophysiological recordings of the treated vs. non-treated cells rigorously were taken in pairs of one treated and one nontreated coverslip within a time frame of 48 hours.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 16:58:16 GMT 2023
by
admin
on
Sat Dec 16 16:58:16 GMT 2023
|
Record UNII |
BH3B64OKL9
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Brand Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C93038
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
||
|
FDA ORPHAN DRUG |
18186
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
||
|
FDA ORPHAN DRUG |
214205
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
||
|
FDA ORPHAN DRUG |
104497
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
||
|
EMA ASSESSMENT REPORTS |
FAMPYRA (AUTHORIZED: MULTIPLE SCLEROSIS)
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
||
|
EU-Orphan Drug |
EU/3/07/458
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
||
|
NDF-RT |
N0000192795
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
||
|
FDA ORPHAN DRUG |
713019
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
||
|
LIVERTOX |
NBK548455
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
||
|
WHO-ATC |
N07XX07
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
||
|
WHO-VATC |
QN07XX07
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
||
|
EPA PESTICIDE CODE |
69201
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
1162454
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
7283
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
1727
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
BH3B64OKL9
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
m4072
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | Merck Index | ||
|
6037
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
4-aminopyridine
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
2416
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
100000081574
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
4163
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
C76777
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
FF-74
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
DTXSID0023870
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
15041
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
Dalfampridine
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
504-24-5
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
207-987-9
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
D015761
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
BH3B64OKL9
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
SUB07505MIG
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
34385
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
DB06637
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
4-AMINOPYRIDINE
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
CHEMBL284348
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | |||
|
897018
Created by
admin on Sat Dec 16 16:58:19 GMT 2023 , Edited by admin on Sat Dec 16 16:58:19 GMT 2023
|
PRIMARY | RxNorm |
Related Record | Type | Details | ||
---|---|---|---|---|
|
BINDER->LIGAND |
BINDING
|
||
|
TARGET -> AGONIST | |||
|
TARGET -> AGONIST | |||
|
TARGET -> AGONIST | |||
|
TARGET -> AGONIST | |||
|
TARGET -> AGONIST | |||
|
TARGET -> AGONIST | |||
|
TARGET -> AGONIST | |||
|
TARGET -> AGONIST |
|
||
|
TARGET -> AGONIST | |||
|
TARGET -> AGONIST | |||
|
SALT/SOLVATE -> PARENT |
|
||
|
EXCRETED UNCHANGED |
URINE
|
||
|
TARGET -> AGONIST | |||
|
METABOLIC ENZYME -> SUBSTRATE |
MAJOR
|
||
|
TARGET -> AGONIST |
|
||
|
TARGET -> AGONIST | |||
|
TARGET -> AGONIST | |||
|
TARGET -> AGONIST |
Related Record | Type | Details | ||
---|---|---|---|---|
|
METABOLITE INACTIVE -> PARENT |
MAJOR
|
||
|
METABOLITE INACTIVE -> PARENT |
MAJOR
URINE
|
Related Record | Type | Details | ||
---|---|---|---|---|
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
|
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |
|
Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
---|---|---|---|---|---|---|
Tmax | PHARMACOKINETIC |
|
|
|||
Volume of Distribution | PHARMACOKINETIC |
|
|
|||
Biological Half-life | PHARMACOKINETIC |
|
|
|||